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1
SFB Molekulare Bioenergetik -Teilprojekt P27
Primary Photoreactions of Membrane Proteins in
Energy and Signal Transduction Application

Josef Wachtveitl
Non-photochemical quenching in LHC-II The
recently obtained high resolution structures of
LCH-II complexes 1,2 provide detailed insight
into the molecular organization of the major
light harvesting protein in plants and should be
complemented with a dynamical picture for a
fundamental understanding of photosynthesis on a
molecular scale. The down-regulation of
photosynthetic light harvesting in excess light
is mainly achieved via the NPQ-mechanism. The
central process is the formation of zeaxanthin
(Zea) from violoxanthin (Vio) by deepoxidation in
the so called xanthophyll cycle.
Xanthophyll cycle
Outlook In order to unambiguously prove the
proposed mechanism, we want to investigate
isolated LHC-II complexes which are enriched in
Zea (Zea-LCH-II) and compare the energy transfer
dynamics with Vio containing LHC-II by ultrafast
spectroscopy. Upon excitation of the lowest
excited singlet state of Chl (QY), we plan to
record the kinetics in the carotenoid radical
cation band in the NIR region (900 - 1100nm).
These experiments represent a critical test of
the quenching mechanism proposed in 1, which
assumes that excitation energy from bulk LHC-II
Chl is transferred (very likely via Chl 8) to
Zea, where it is trapped and nonradiative
dissipation remains as the only decay channel.
The qE quenching scheme, which present generation
of Zea, upon selective excitation of bulk Chl Qy
band at 664 nm is presented below .
Energy level diagram of carotenoids and
chlorophylls
P7 (Kühlbrandt) biochemical experiments and the
structural determinations P29 (Dreuw) quantum
chemical calculations of NPQ
Photosynthetic excitation energy transfer in
FCPs Fucoxanthin-chlorophyll protein (FCP), the
peripheral light-harvesting complex in diatoms
exhibits a high sequence homology with the LHC-II
complex of green plants, but differs
substantially in its pigment composition 3,
employing carotenoids rather than chlorophylls
for the capturing of sunlight.
Future plans The ultrafast excitation energy
transfer to Chl a following the photoexcitation
of fucoxanthin (S0?S2 transition) shall be
studied by vis/near-IR and vis/mid-IR pump-probe
experiments. We hope to establish a time scale
for the various Car-Chl and Chl-Chl energy
transfer reactions in a mode sensitive way.
This light harvesting antenna binds Chl a,
fucoxanthin and Chl c molecules in a 441 ratio.
Upon excitation of the carotenoid to its S2
state, a significant path of the excitation
energy is transferred very fast to Chl a.The
energy transfer dynamics that takes place in FCP
will be investigated, knowing that the
combination of fucoxanthin with a
multi-chlorophyll system results into efficient
light harvesting.
P28 (Büchel) biochemical work and the structural
analysis P24 (Hellwig) spectroscopic studies in
the far-IR P29 (Dreuw) QM calculation of a model
for singlet and triplet energy transfer
Primary reactions of proteorhodopsin The
structural dynamics of retinal proteins,
especially details of the initial
photoisomerization of the chromophore is an area
of intense efforts. At present, several different
models are discussed. The ambiguities are
partially due to a lack of experimental time
resolution. We therefore plan to study the
photodynamics of wild type and mutant
proteorhodopsin as well as channelopsin with
highest time resolution.
Electron transfer in cytochrome c552 For the
photoinitiation of electron transfer in
cytochrome c552 we plan the design and the
spectroscopic characterization of ruthenium
complexes C552/ruthenium. The soluble domain of
this protein is ideally suited for these studies,
since the structure is known for both
redox-states 4. The ruthenium-labelled
cytochrome c552 is also an excellent model system
for the study of electron transfer induced
folding/unfolding dynamics 5. This project
requires electrochemical techniques and will thus
be carried out in close cooperation with These
experiments have already been proposed for the
current funding period, but were delayed due to
availability problems of the suitable ruthenium
reagent and difficulties with the coupling
reaction.
As in similar experiments with ultrashort pulses
we expect to detect oscillatory contributions,
reflecting wave packet dynamics on the excited
state potential energy surface. This approach to
extract vibrational information from electronic
spectra shall be complemented by the recently
completed fs mid-IR spectroscopy setup (see P27
report). In 2006 we plan to set up a broadband
fs-fluorescence experiment. In collaboration with
the Munich group we could already show that this
technique also complements fs time resolved
absorption experiments and allows detailed
observation of the excited state dynamics of
retinal proteins.

primary proton donor
primary proton acceptor
P21 (Mäntele) P24 (Hellwig) P8 (Ludwig).
molecular model of proteorhodopsin T. Friedrich
et al. (2002) JMB, 321, 821
P1 (Bamberg) electrophysiological studies
Does the replacement of Asp97 by Asn confirm the
pH dependent measurements (see P27 report)?
Photoinduced dynamics in QFR The enzyme
quinolfumarate reductase (QFR) from the
anaerobic e-proteobacterium Wolinella
succinogenes is part of the anaerobic respiratory
system of this organism. It couples the reduction
of fumarate to succinate to the oxidation of
menaquinol to menaquinone. The three-dimensional
structure of the Wollinella succinogenes QFR 6
revealed the exact location of the two heme b
groups (bP and bD) within the hydrophobic subunit
C. These two hemes are actively involved in the
electron transfer reactions driving succinate
oxidation and quinone reduction, their proximity
and spectral properties make them ideal
candidates for optical spectroscopic studies.
Layout of the proposed femtosecond fluorescence
(Kerr sutter Technique)
Using ultrafast spectroscopy with selective
excitation of the hemes, we would like to
investigate the interactions between hemes bP and
bD and the differences in this interaction
between the mixed valence and the fully reduced
enzyme (DMNH2 vs. dithionite reduced QFR).
1) Standfuss, J., Terwisscha van Scheltinga,
A.C., Lamborghini, M. and Kühlbrandt, W. (2005)
EMBO J. (in press). 2) Dreuw, A., Fleming, G.R.
and Head-Gordon, M. (2003) Phys.Chem. Chem.
Phys., 5, 32473256. 3) Büchel, C. (2003)
Biochemistry, 42, 13027-13034. 4) Harrenga, A.,
Reincke, B., Rüterjans, H., Ludwig, B. and
Michel, H. (2000) J. Mol. Biol., 295, 667-678.
5) Wittung-Stafshede, P., Lee, J.C., Winkler,
J.R., Gray, H.B. (1999) Proc. Natl. Acad. Sci.
U.S.A., 96, 6587-6590. 6) Lancaster, C.R.D.,
Kröger, A., Auer, M. and Michel, H. (1999)
Nature, 402, 377-385.
First time resolved data acquired from a reduced
QFR sample by exciting the ? band of the hems at
387 nm and probing the ? band transition (530 and
560 nm)
P19 (Lancaster) electron transfer studies of the
diheme center in QFR
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